Canonical Allele Identifier: PA2827020475
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.His1564Arg
CA021150
NM_001318832.2:c.4691A>G